Pharmacokinetics of clarithromycin in the prostate: implications for the treatment of chronic abacterial prostatitis

J Urol. 2001 Jan;165(1):97-9. doi: 10.1097/00005392-200101000-00024.

Abstract

Purpose: We studied the pharmacokinetics of orally administered clarithromycin in prostatic tissue to define its role in the treatment of chronic abacterial prostatitis caused by intracellular pathogens.

Materials and methods: A total of 45 men receiving 3 oral doses of 750 mg. clarithromycin at 12-hour intervals underwent suprapubic prostatectomy for benign prostate hyperplasia 4, 5, 6 and 7 hours after the last drug dose in 13, 12, 10 and 10 patients, respectively. Concentrations were determined in the prostate tissue and in plasma by an agar diffusion assay.

Results: A mean peak level of clarithromycin of 3.22 and 3.08 microg./gm. of tissue was achieved 4 hours after the third drug dose at the center and periphery of the adenoma, respectively. Tissue levels remained statistically superior to plasma levels at all intervals.

Conclusions: The oral administration of clarithromycin achieved a prostate level much higher than the minimal inhibitory concentration of clarithromycin for the intracellular pathogens of chronic prostatitis. Thus, clarithromycin may be considered for treating chronic abacterial prostatitis.

MeSH terms

  • Administration, Oral
  • Aged
  • Anti-Bacterial Agents / pharmacokinetics*
  • Anti-Bacterial Agents / therapeutic use
  • Chronic Disease
  • Clarithromycin / pharmacokinetics*
  • Clarithromycin / therapeutic use
  • Humans
  • Male
  • Prostate / metabolism
  • Prostatectomy
  • Prostatic Hyperplasia / surgery
  • Prostatitis / drug therapy*
  • Time Factors
  • Tissue Distribution

Substances

  • Anti-Bacterial Agents
  • Clarithromycin